Canonical Allele Identifier: CA385543346

Gene: CDK4 TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57749252G>T , CM000674.2:g.57749252G>T	GRCh38
NC_000012.11:g.58143035G>T , CM000674.1:g.58143035G>T	GRCh37
NC_000012.10:g.56429302G>T	NCBI36
NG_007484.2:g.8130C>A , LRG_490:g.8130C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.749C>A (CDK4) MANE Select	ENSP00000257904.5:p.Pro250His
ENST00000257910.8:c.*1962G>T (TSPAN31) MANE Select	ENSP00000257910.3:n.*1962G>T
ENST00000257904.10:c.749C>A (CDK4)	ENSP00000257904.5:p.Pro250His
ENST00000312990.10:c.*61C>A (CDK4)	ENSP00000316889.6:n.*61C>A
ENST00000546489.5:c.527C>A (CDK4)	ENSP00000447779.1:p.Pro176His
ENST00000547281.5:c.527C>A (CDK4)	ENSP00000447274.1:p.Pro176His
ENST00000547992.5:c.*1962G>T (TSPAN31)	ENSP00000448209.1:n.*1962G>T
ENST00000549606.5:c.-41C>A (CDK4)	ENSP00000447005.1:n.-41C>A
ENST00000550419.5:c.*155C>A (CDK4)	ENSP00000448098.1:n.*155C>A
ENST00000551888.5:n.575C>A (CDK4)
ENST00000552713.5:n.408C>A (CDK4)
ENST00000553237.5:c.*388C>A (CDK4)	ENSP00000448885.1:n.*388C>A
NM_000075.3:c.749C>A (CDK4)	NP_000066.1:p.Pro250His
NM_000075.4:c.749C>A (CDK4) MANE Select	NP_000066.1:p.Pro250His
NM_005981.5:c.*1962G>T (TSPAN31) MANE Select	NP_005972.1:n.*1962G>T
NM_001330168.2:c.*1962G>T (TSPAN31)	NP_001317097.1:n.*1962G>T
NM_001330169.2:c.*1962G>T (TSPAN31)	NP_001317098.1:n.*1962G>T